FDAFDA · Food and drugs·Recall number Z-1003-2026
Philips Incisive CT
Published January 14, 2026 · Recall initiated: December 3, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Potential for incomplete scan due to unstable connection inside of floating sensor.
What to do
FDA Mandated
Recall details
- Manufacturer
- Philips Healthcare (Suzhou) Co., Ltd.
- Distributor
- U.S. and U.S. territories
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- China
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